Canonical Allele Identifier: CA2410885350

Gene: MIOX

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50489826C= , CM000684.2:g.50489826C=	GRCh38
NC_000022.10:g.50928255C= , CM000684.1:g.50928255C=	GRCh37
NC_000022.9:g.49275121C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000216075.11:c.828C= MANE Select	ENSP00000216075.6:p.Asp276=
ENST00000216075.10:c.828C=	ENSP00000216075.6:p.Asp276=
ENST00000395732.7:c.*1C=	ENSP00000379081.3:n.*1C=
ENST00000395733.7:c.*1C=	ENSP00000379082.3:n.*1C=
ENST00000451761.1:c.768C=	ENSP00000409894.1:p.Asp256=
NM_017584.5:c.828C=	NP_060054.4:p.Asp276=
XM_005261925.3:c.690C=	XP_005261982.1:p.Asp230=
XR_244455.2:n.3324C=
XM_005261925.4:c.690C=	XP_005261982.1:p.Asp230=
NM_017584.6:c.828C= MANE Select	NP_060054.4:p.Asp276=